Fe-Cu duplex metal filaments

ABSTRACT

Metal filaments are grown by solid state reactions from a matrix or matte of copper, iron and sulfur. Copper filaments, iron filaments or copper-iron duplex filaments may be produced by adjustment of temperature and growth conditions. The copper-iron duplex filaments consist of copper at one end and iron at the other with a sharp junction between the two compositions. Individual filaments are typically on the order of 1 micron in diameter and the filaments grow in bundles often about 10 microns in diameter. Growth is extremely rapid; lengths of 2 to 3 centimeters being attained in a few minutes.

Leavenworth, Jr. et al.

Sept. 2, 1975 [54] Fe-Cu DUPLEX METAL FILAMENTS [75] lnventors: Howard W. Leavenworth,Jr.,

Washington, DC; Beverly W. Dunning, Jr., Adelphi, Md.; Robert C. Gabler, Jr., Grasonville, Md.; Carl E. Goldsmith, Brandywine, Md.

[73] Assignee: The United States of America as represented by the Secretary of the Interior, Washington, DC.

[22] Filed: Sept. 25, 1974 [21] Appl. No.: 509,152

Related US. Application Data [62] Division of Ser. No. 359,400, June 25, 1973.

[52] U.S. Cl 29/19l.6; 29/192 R; 29/1963; 75/.5 BA; 75/.5 R [51] Int. Cl. B22F 9/00 [58] Field of Search 29/l9l.6, 192 R, 196.3; 75/DlG. l, .5 R, .5 BA

[56] References Cited UNlTED STATES PATENTS 3.060.013 10/1962 Harvey... 75/DIG. 1 3,529,954 9/1970 Ccch 75/.5 B

FOREIGN PATENTS OR APPLICATIONS 1,729 8/1973 Netherlands 29/1911) OTHER PUBLICATIONS Ceramic Fibers and Fibrous Composite Materials, Rauch et al., Academic Press, 1968, p. 218.

Primary Examiner-C. Lovell Assistant Examiner-Arthur J. Steiner Attorney, Agent, or FirmRoland H. Shubert; Donald R. Fraser [5 7 ABSTRACT Metal filaments are grown by solid state reactions from a matrix or matte of copper, iron and sulfur. Copper filaments, iron filaments or copper-iron duplex filaments may be produced by adjustment of temperature and growth conditions. The copper-iron duplex filaments consist of copper at one end and iron at the other with a sharp junction between the two compositions. Individual filaments are typically on the order of 1 micron in diameter and the filaments grow in bundles often about 10 microns in diameter. Growth is extremely rapid; lengths of 2 to 3 centimeters being attained in a few minutes.

3 Claims, 1 Drawing Figure PATENTED IP 2 I975 COPPER DEPLETED MATTE COPPER SULFER IRON Io II I l2 MELT LIQUID COOL SOLID MATTE CRUSH l9 o 300 TO 450C 600 C cu FILAMENTS Fe FILAMENTS SEPARATE SEPARATE 22 21 24 28% COPPER IRON FILANIENTS FILAMENTS IRON -,-DEPLETED MATTE Fe-Cu DUPLEX METAL FILAMENTS This is a division of application Ser. No. 359,400, filed June 25, 1973, now US. Pat. No. 3,852,060.

BACKGROUND OF THE INVENTION Very fine metal filaments commonly have extremely high strengths and other unusual physical properties. Such filaments have often been incorporated into a matrix, such as another metal, to impart greater strength or other desirable physical characteristics to the composite.

Metal filaments have been grown in the past from metal alloy compositions in which one component of the alloy is caused to grow as a filament under the influence of high temperatures and thermal gradients. An example of this technique as applied to the growth of copper filaments is found in U.S. Pat. No. 3,060,013.

SUMMARY OF THE INVENTION When copper, iron, and sulfur are heated together, there is formed a matte which contains a variety of copper and iron sulfides and usually some free or elemental metals depending upon the proportions of the matte. If the matte is stoichiometrically deficient in sulfur, that is, if less sulfur is present than that required to satisfy the requirements of the copper and iron for the formation of simple sulfides, then the sulfur will partition between the iron and copper in the solid matte. Simple sulfides are defined for the purposes of this disclosure as CuS and FeS. Depending upon temperature, the sulfur will partition with the copper leaving free iron or will partition with the iron leaving free copper. When such a sulfur deficient matte is crushed so as to create a large surface area and is thereafter heated in a nonreactive atmosphere, filaments of copper or iron grow outwardly from the surfaces of the matte particles. The filaments easily break free from the matte surfaces and may be separated from the metal-depleted matte by conventional techniques.

Hence, it is an object of our invention to produce metal filaments.

It is another object of our invention to extract metals in the form of filaments from sulfide mattes.

Another object of our invention is to grow iron filaments and copper filaments.

Yet another object of our invention is to produce copper-iron duplex filaments.

BRIEF DESCRIPTION OF THE DRAWINGS For a fuller understanding of the invention, reference is made to the following description taken in connection with the accompanying drawing in which:

The single FIGURE shows schematically the process for producing metal filaments described in this specification.

DETAILED DESCRIPTION OF THE INVENTION We have found that copper, iron, or copper-iron duplex filaments may be readily grown from a solid matte of copper, iron, and sulfur which is stoichiometrically deficient in sulfur. Filament growth is extremely rapid; growth rates of 2 to 3cm in 5 minutes being commonplace. Filament growth requires a nonreactive atmosphere which may be an inert gas such as nitrogen or a vacuum. The vacuum need not be good, 0.05 Torr or less will sufficc. but care must be taken to insure that the atmosphere will not oxidize metalsat the surface of the matte and that iron carbides do not form as will occur if oil from a vacuum pump is allowed to contaminate the matte. If either oxides or carbides form on the matte surfaces, filament growth will stop.

Depending upon the temperatures, either copper filaments or iron filaments may be grown from matte surfaces. The filaments grow outwardly from the matte surfaces as bundles of fibers. Individual filaments or fibers are typically slightly less than 1 micron in diameter and filament bundles are usually about 10 microns in diameter. A temperature gradient is not necessary for filament growthdHowever, a temperature gradient will cause orientation of the growing filaments causing them to grow toward the cold area.

Referring now to the FIGURE, copper l0, sulfur 1 l, and iron 12 are melted in heating means or furnace 13. All three components may be in their elemental form or may be added in the form of either copper or iron sulfides or both. The metal sulfides may be in the form of ore concentrates such as ehalcopyrite (CuFeS 'as a mixture of covellite (CuS), and pyrite a marcasite (FeS or as combinations of other copper, iron, or copper-iron sulfides, or as combinations of metals and metal sulfides. Impurities, such as the normal gangue constituents of sulfide ore concentrates, do not normally interfere with the process.

An ore concentrate, such as ehalcopyrite, is not stoichiometrically deficient in sulfur. Upon heating ehalcopyrite to a relatively high temperature, above about 800C, some elemental sulfur is driven off. This is best accomplished in a vacuum furnace provided with a condenser to collect the evolved sulfur. Heating a chalcopyrite concentrate to a temperature of 800C for 2 hours in a vacuum furnace results in a lowering of the sulfur content from about 32% to about 27% to form a sulfur deficient matte from which filaments may be grown. Pyrite will also decompose with the evolution of free sulfur at these temperatures.

While it is not absolutely necessary to melt the mixture of copper, iron, and sulfur provided the three components are in intimate physical admixture, a melting step to prepare the sulfur deficient matte is strongly preferred. A melting Step introduces a number of advantages to the process even when using a copper-iron sulfide such as ehalcopyrite as the raw material. Melting ehalcopyrite will drive off along with the sulfur most of the sulfides of lead, zinc, and the alkali metals which tends to purify the matte and allows recovery of valuable metals associated with the ehalcopyrite. Further, melting a ehalcopyrite charge and allowing it to cool as an ingot or within the furnace results in the formation of a siliceous slag whichsolidifies above the matte. This slag layer cleanly separates from and does not adhere to the matte, thus allowing its separation after cooling. As a result, the matte is further concentrated and purified.

When iron, copper, or sulfur are added in a physical form which precludes intimate mixing with the other components, then melting the components to form a matte becomes a necessity. Metallic iron may be added in the form of scrap such as shredded sheet or can stock; copper may be added in the form of wire or other scrap forms, and sulfur may be added as a solid or liquid or in the form of a metal sulfide. Dissolution of copper or iron in sulfur is rapid at high temperatures. Temperature level required to form a molten matte is above about 900C. Chalcopyrite, which can be considered an equimolar mixture of cupric sulfide (covcllite) and ferrous sulfide (troilite) melts at about 915C, and this represents about the minimum temperature at which a matte deficient in sulfur may be melted since the melting point increases as sulfur content decreases.

A liquid, sulfur deficient matte 14, is allowed to solidify and cool in zone 15. Composition of the sulfur deficient matte 14 may broadly range from to 30 weight sulfur, 20 to 50 weight iron, and 30 to 60 weight copper. A more preferred matte composition contains from 15 to 25 weight sulfur, 25 to 40 weight iron and 40 to 55 weight copper. Our most preferred matte composition contains from 16.5 to 21.5 weight sulfur, 32.5 to 37.5 weight iron, and 42.5 to 47.5 weight copper. While copper and iron filaments can be grown at the extremes of these composition ranges, yield of filaments increases substantially as the matte composition approaches and enters the most preferred range. As was explained previously, zone 15 may comprise the furnace itself or may be an ingot mold or similar device. After cooling to below about 300C and preferably to near ambient temperatures, solid matte 16 is removed from cooling zone 15 and is crushed to form relatively fine particles in means 17. Purpose of the crushing step is to create a large surface area from which the metal filaments can grow. Particle size of the crushed matte is not critical but a size range of approximately -5+2O mesh works well in the process.

Crushed matte from zone 17 may be used to grow either copper filaments, iron filaments, or in some cases both. When it is desired to grow copper filaments, a crushed matte fraction 18 is passed to heating means 19. Means 19 comprises a closed device having temperature control capabilities. Filament growth requires a nonreactive atmosphere which may either be an inert gas or vacuum. Hence, means 19 may comprise a temperature controlled vacuum furnace, oven, or similar device. Upon heating the matte particles to a temperature within the range of about 300 to 450C., copper filaments grow upon the matte surfaces. It is not necessary to precisely control the temperature during filament growth since temperature variations within the growth range appear to affect only the rate of filament growth. A preferred temperature range for copper filament growth is between 375 and 425C.

When it is desired to grow iron filaments, crushed matte fraction 20 from means 17 is passed to heating means 21. Means 21 may be similar to or identical with means 19 except that means 21 must be capable of maintaining a higher temperature. lron filament growth occurs at a temperature above about 600C but below the melting point of the matte. It is preferred that the growth temperature for iron filaments be within the range of 600 to 700C. Little advantage is gained by exceeding 700.

In order to understand why both iron and copper fila- A perature, the reaction tends to proceed to the left. Hence, metallic copper is formed at relatively low temperatures, while metallic iron is formed at somewhat higher temperatures. Exactly why and how the metallic iron or copper grows in the form of filaments from the matte surfaces is not fully understood.

After filament growth is complete, a matte fraction 22, having copper filaments adhering to the surface of the matte particle, is passed to separation zone 23. In zone 23, filaments may be detached from the matte by tumbling the matte particles as the filaments readily break free of the matte surface. Filaments 24 may then be separated from matte particles by screening, air elutriation, tabling, or similar conventional methods. A recycle matte stream 25, depleted in copper, may be recycled to melt zone 13 to provide at least part of the iron and sulfur requirements of the process.

When growing iron filaments, the recovery procedure is somewhat more critical. After iron filament growth is complete, a matte fraction 26, having iron filaments adhering to the surface of the matte particles, is passed to separation zone 27. At this point, extra precautions must be taken in recovering iron filaments compared to those taken in the recovery of copper filaments. Growth of the iron filaments must be stopped as the matte particles are removed from growth zone 21. This is most easily accomplished by rapidly cooling the matte particles to a temperature below about 300C. If the matte particles are cooled slowly through the transformation temperature of about 475C, iron filaments redissolve into the matte. Upon further cooling to a temperature within the range of about 300 to 450C, copper filaments will start to grown. Growth of the copper filaments occurs below the base of the iron filaments to form a duplex filament, iron on one end and copper at the other with a sharply defined junction between the two sections. In like fashion, if copper filaments are grown upon matte particles and the temperature is raised above the transformation temperature of about 475C, to a level of about 525C for example, copper filaments are redissolved into the matte. Raising the temperature even higher, to 600C or above, before copper filaments are completely redissolved causes iron filaments to grow under the base of the copper filaments, thus, again producing a copper-iron duplex filament. These duplex filaments display interesting physical and electrical characteristics and may find use in electronic components, miniature thermocouples, and the like as well as being useful generally in other applications where fine wires and filaments presently are employed.

But in order to recover iron filaments in good yield, it is necessary to stop the filament growth-filament dissolution mechanism. This is most easily accomplished by cooling the matte particles and attached filaments at a rate sufficiently rapid so as to prevent iron filament dissolution and growth of copper filaments. Cooling of the filaments and surfaces of the matte particles to temperature levels below about 300C must be accomplished in substantially less time then required for filament growth. In practical terms, cooling must be accomplished within a minute or so but preferably even faster. Cooling may readily be accomplished by subjecting the matte particles to a flowing stream of relatively cold inert gas. It is also possible to stop filament growth and prevent dissolution of the filaments by introducing small quantities or a reactive gas such as air into the growth chamber. This method is less favored because filament surfaces are also affected.

lron filaments may be detached from matte particles in zone 27 by tumbling or other mild physical treatment. The filaments may then be easily separated from 'the matte by magnetic means or by other physical separation techniques, such as those used with copper filaments, to recover an iron filament fraction 28. An irondepleted matte fraction 29 may be recycled back to melt zone 13 to provide at least a part of the sulfur and copper requirements for the process.

The following examples will serve to more thoroughly illustrate specific embodiments of our invention.

EXAMPLE 1 A chalcopyrite flotation concentrate was obtained which assayed 28.4% copper, 28.0% iron, 3 l .9% sulfur, 0.60% zinc, 0.06% lead, 0.3% molybdenum, 0.43% calcium oxide, and 7.0% insoluble. All values are in weight percent. In addition, the concentrate assayed 0.003 ounces gold and 3.3 ounces silver per ton. Spectrographic analysis showed the presence of silicon and aluminum in significant amounts and small quantities of titanium, bismuth, manganese, barium, cobalt, lithium, nickel, and strontium.

A sample of the chalcopyrite concentrate was heated in a vacuum furnace equipped with a condenser. Evolution of free sulfur began at a temperature of about 500 to 550C. The furnace charge was raised to a maximum temperature of 800C and held at that temperature for about 2 hours or until all sulfur evolution ceased. Sulfur content of the matte produced was about 27% compared to an original concentration of about 32%.

Another charge of the chalcopyrite concentrate was melted in the vacuum furnace. some free sulfur and a number of different metal sulfides including lead sulfide, zinc sulfide, and alkaline sulfides were condensed and collected on the condenser surfaces. some Mo and Ag sulfides were entrained by the other volatile sulfides but for the most part they remained with the matte. Upon cooling, a silica slag formed above a Cu-Fe-S matte. The slag layer did not adhere to the matte and was easily removed. Additional melting tests of the same ore concentrate were performed and the sulfur content of the recovered mattes ranged from about 27 to 30%. It was observed that neither prolonged heating above the melting point nor raising the temperature to as high as 1450C had a significant effect upon the sulfur content of matte compositions produced.

EXAMPLE 2 Sulfur deficient mattes produced in Example 1 were cooled to ambient temperature and crushed to a relatively small particle size. The matte particles were then heated in a vacuum to temperatures in the range of about 350 to 430C. Copper filaments grew from the surfaces of the matte particles. Maximum filament growth was obtained in about half an hour at 350C and in much shorter times at 430C. The matte particles and copper filaments were then cooled to ambient conditions in the vacuum. Copper filaments were detached from the matte particles by tumbling and a copper filament fraction was recovered by screening. The copper filaments analyzed over 99.3?! copper metal and the impurities appeared to be derived from small amounts of matte contamination.

I EXAMPLE 3 A sulfur deficient matte similar to those produced in Example 1 was crushed and the matte particles were then rapidly heated in a vacuum to a temperature of about 625C. Iron filaments grew upon the matte surfaces. Lowering the temperature to a level below about 475C, caused the iron filaments to redissolve into the matte. Raising the temperature to about 625C caused iron filaments to again grow upon the matte surfaces. Rapid cooling of the matte and associated iron filaments to a temperature below about 300C prevented dissolution of the filaments and allowed their later recovery.

EXAMPLE 4 A sulfur deficient matte, similar to those produced in Example 1, was crushed and the matte particles were heated in a vacuum to a temperature of about 400C. Copper filaments grew upon the matte surfaces. The matte and copper filaments were then heated to about 525C whereupon the filaments were redissolved into the matte. The temperature of the matte was then lowered to 400C and copper filaments once again grew from the matte.

Rapid heating of the matte particles and attached copper filaments to a temperature of about 625C resulted in little if any dissolution of the copper filaments but upon holding the matte particles at 625C for a few minutes, iron filaments began to grow beneath and attached to the copper filaments. The matte and attached filaments were then rapidly cooled to a temperature below about 300C and there was recovered from the matte copper-iron duplex filaments.

EXAMPLE 5 Examples 2 and 3 were repeated using a nitrogen atmosphere rather than a vacuum. Essentially identical results were obtained.

EXAMPLE 6 A sulfur deficient matte was obtained by heating a pelletized homogeneous mixture of elemental iron, copper, and sulfur to a temperature of about 800C. This matte was then used to grow both iron and copper filaments. Essentially equivalent results were obtained using this matte as were obtained by use of the mattes of Example 1.

EXAMPLE 7 Shredded tin cans were added to a copper sulfide material and the mixture was melted to form a Cu-Fe-S matte deficient in sulfur. The cans were not de-tinned prior to use. This matte was then used to grow both iron and copper filaments. It was found that metallic tin tended to vaporize from the matte when iron filaments were grown in a vacuum environment and that the tin tended to inhibit filament growth. However, tin did not interfere with the growing of copper filaments nor did it interfere with the growing of iron filaments when iron filament growth was conducted in a nitrogen atmosphere rather than in a vacuum.

EXAMPLE 8 A particle of matte was placed in an evacuated quartz tube which was then inserted horizontally into a muffle furnace held at 400C. One end of the quartz tube extended to the exterior of the furnace which was at ambient temperature. Thus, there was created a temperature gradient over the length of the tube.

Copper filaments grew quickly from the matte. Filaments were long and straight and grew toward the cold end of the tube. No filaments formed on the side of the matte particle facing the hot end of the tube. In con trast, heating matte particles uniformly without a temperature gradient resulted in filaments growing in random directions and sometimes becoming entangled.

As may be appreciated, our invention may also be viewed as a metallurgical process to extract copper, iron, or both from their sulfide ores. It may also be used ing a diameter on the order of about 10 microns.

* l l l 

1. A COPPER-IRON DUPLEX FILAMENT CONSISTING OF IRON AT ONE END AND COPPER AT THE OTHER END WITH A SHARPLY DEFINED JUNCTION BETWEEN THE TWO SECTIONS, SAID FILAMENT HAVING A DIAMETER ON THE ORDER OF 1 MICRON.
 2. The filament of claim 1 having a length greater than 1 centimeter.
 3. The filament of claim 1 wherein multiple filaments are arranged in the form of bundles, said bundles having a diameter on the order of about 10 microns. 